Thermoplastic foams and method of forming them using nano-graphite

ABSTRACT

Rigid foam insulating products and processes for making such insulation products are disclosed. The foam products are formed from a polymer, a blowing agent, and nano-graphite. The nano-graphite has a size in at least one dimension less than about 100 nm and, in exemplary embodiments may be an intercalated, expanded nano-graphite. In addition, the nano-graphite may include a plurality of nanosheets having a thickness between about 10 to about 100 nanometers. The nano-graphite acts as a process additive to improve the physical properties of the foam product, such as thermal insulation and compressive strength. In addition, the nano-graphite in the foam controls cell morphology and acts as a nucleating agent in the foaming process. Further, the nano-graphite exhibits overall compound effects on foam properties including improved insulating value (increased R-value) for a given thickness and density and improved ultraviolet (UV) stability.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of prior applications U.S. patentapplication Ser. No. 10/722,929 entitled “Method Of FormingThermoplastic Foams Using Nano-Particles To Control Cell Morphology”filed on Nov. 26, 2003, and U.S. patent application Ser. No. 11/481,130entitled “Polymer Foams Containing Nano-Graphite” filed on Jul. 5, 2006,which is a continuation-in-part of U.S. patent application Ser. No.11/026,011 entitled “Polymer Foams Containing Nano-Graphite” filed Dec.31, 2004 (now U.S. Pat. No. 7,605,188), the entire contents of each ofwhich are expressly incorporated herein.

TECHNICAL FIELD AND INDUSTRIAL Applicability of the Invention

The present invention relates generally to foam products, and moreparticularly, to rigid foamed polymeric boards containing nano-graphite.The nano-graphite is added to provide benefits as a process aid, anR-value enhancer, UV radiation stability enhancer, a dimensionalstability enhancer, a mechanical strength enhancer, and as a fireretardant. The added nano-graphite also is added to reduce foam surfacestatic, to function as internal lubricant in the foaming process, and tocontrol the cell morphology. A wide range of cell morphologies may beobtained by utilizing nano-particles as nucleating agents. Such rigidfoams are useful for forming rigid insulating foam boards suitable inmany conventional thermal insulation applications.

BACKGROUND OF THE INVENTION

In the past, infrared attenuating agents (IAAs) such as carbon blackpowdered amorphous carbon, graphite, and titanium dioxide have been usedas fillers in polymeric foam boards to minimize material thermalconductivity which, in turn, will maximize insulating capability(increase R-value) for a given thickness. R-value is defined as thecommercial unit used to measure the effectiveness of thermal insulation.A thermal insulator is a material, manufactured in sheets, that resistsconducting heat energy. Its thermal conductance is measured, intraditional units, in Btu's of energy conducted times inches ofthickness per hour of time per square foot of area per Fahrenheit degreeof temperature difference between the two sides of the material. The Rvalue (per inch) of the insulator is defined to be 1 divided by thethermal conductance per inch. R is an abbreviation for the complex unitcombination hr·ft²·° F./Btu. In SI units, an R value of 1 equals 0.17611square meter Kelvin per watt (m²·K/W).

The heat transfer through an insulating material can occur through solidconductivity, gas conductivity, radiation, and convection. The totalthermal resistance, R, (sometimes called R-value) is the measure of theresistance to heat transfer, and is determined as: R=t/k, where,t=thickness.

Rigid foamed plastic boards are extensively used as thermal insulatingmaterials for many applications. It is highly desirable to improve thethermal conductivity without increasing the density, and/or thethickness of foam product. Particularly, the architectural communitydesires a foam board having a thermal resistance value of R=10, with athickness of less than 1.8″, for cavity wall construction, to keep atleast 1″ of the cavity gap clean.

It is also desirable to improve the UV stability, particularly for suchas exterior wall insulation finishing system (EIFS), and highway andrailway underground applications where prolonged exposure of sun lightof the surface of the polymer foam boards are usually occurred injob-sites.

The physical properties of rigid polymer foam boards, such as theircompressive strength, thermal conductivity, dimensional stability, waterabsorption rate, depend in large part on the micro-structure of thematerial forming the boards, i.e., the cell morphology of the foam.However, it can be difficult to control polymer foaming to the degreenecessary for consistent production of a desirable cell morphology thatwill tend to optimize the overall foam properties, or to improve aspecific property, such as the thermal insulation value of the foam

Prior art attempts to make foam micro-structures having desirable cellmorphologies have included the use of nucleation agents such as powdersformed from inorganic oxides, various organic materials and metals.Among these nucleation agents, the inorganic oxides, such as talc,titanium dioxide and kaolin, are the most commonly used. The size,shape, particle distribution and surface treatment of the nucleationagent(s) utilized in the process to form a foam will all tend to affectthe nucleation efficiency and, consequently, the cell size morphologyand distribution in the resulting foam.

Conventional methods for controlling the cell morphology, however, tendto be limited by difficulties in evenly distributing particles of thenucleation agent throughout the polymer and/or suppressing coagulationof the dispersed particles. Certain structural defects in the resultingfoams are generally attributed, at least in part, to dimensionaldifferences between the particles of the nucleating agents, which may bein the range of several microns, particularly in situations where therehas been some degree of coagulation, and the desired cellmicrostructures, which may have a target cell wall thickness in therange of 0.2 to 6 microns, often one micron or less, for low densitycommercial insulation foams.

This size difference between the nucleation agent particles and the cellwall thickness may also result in relatively weak interactions betweenthe nucleating agent and nano-scale polymer, thereby weakening theoverall foam structure. Similarly, cell defects may also be attributed,at least in part, to the hydrophilic surface of most conventionalinorganic nucleation agents that makes them difficult to disperse evenlyin a polymer. These effects tend to result in processing difficulties,such as corrugation of the resulting foam board, when nucleation agentsare added at levels greater than about 2 weight percent or the mediancell size of the resulting foam is less than around 120 microns.

Prior art attempts to avoid foam structure corrugation effects haveutilized cell size enlarging agents such as the waxy compositionsdisclosed in U.S. Pat. No. 4,229,396, the contents of which are herebyincorporated by reference in their entirety, and the non-waxycompositions disclosed in U.S. Pat. No. 5,489,407, the contents of whichare hereby incorporated by reference in their entirety.

Another effort directed toward foam structures having bi-modal cellmorphology (Kanelite Super EIII, Kaneka, Japan) included use ofimmiscible blowing agents, such as water and hydrocarbon. Thiscombination, however, tends to result in processing difficulties due tothe low solubility of water in the polymer and the reaction of waterwith fire retardant, such as hexabromocyclododecane (HBCD) at theelevated temperatures typically utilized during the extrusion process.

Thus, there is a need for foam products, more specifically rigid foamboards, utilizing nano-graphite particles having at least onedimension—usually the thickness of the plate shaped graphite innano-scale, i.e., less than 0.1 microns or 100 nanometers. It is afurther object of the present invention to provide a process forpreparing low density extruded polymer foams and foam boards containingnano-graphite which has good processing properties, and improved foamphysical properties, including thermal conductivity, ultraviolet (UV)radiation resistance, dimensional stability, mechanical strength, flamespread rate and smoke density.

SUMMARY OF THE INVENTION

The present invention relates to foam insulating products and theprocesses for making such products, such as extruded polystyrene foam,that contains nano-graphite as a process additive to improve thephysical properties such as thermal insulation and compressive strength.During foaming, nano-graphite acts as a nucleating agent and lubricant.Lubrication by the nano-graphite makes the flow of the melted polymer inthe extruder easier, and provides a smooth surface to the foam board.Further, the nano-graphite reduces the amount of static present duringthe foaming process due to the increased electric conductivity of theskin of the nano-graphite polymer foam boards. Nano-graphite in a foamproduct also acts as a UV stabilizer and as a gas barrier in the finalproduct.

The nano-particles (e.g., nano-graphite) are typically particles with atleast one dimension less than 100 nm and may be incorporated into thepolymer as surface modified nano-particles, nano-particles havingmechanochemical bonds to a core micron sized particle, nano-particlecompounds in combination with polymers, such as master batchcompositions, and/or liquid blowing agents. Further, the nano-particlepolymer compounds can be intercalated nano-layers, such as compoundsformed simply by mixing nano-montmorillonite (MMT) or expanded graphitewith a polymer, or exfoliated nano-layers, such as compounds formed bythe in-situ polymerization of polymer precursors in the presence ofnano-MMT or nanosheets or other surface-modified inorganic or graphiteparticles.

It is an object of the present invention to produce a rigid polymer foamcontaining nano-graphite which exhibits overall compound effects on foamproperties including improved insulating value (increased R-value) for agiven thickness and density, and ultraviolet (UV) stability.

It is another object of the present invention to produce a rigid polymerfoam containing nano-graphite having retained or improved compressivestrength, thermal dimensional stability and fire resistance properties.

It is yet another object of the present invention to providenano-graphite in a rigid polymer foam which also acts as a processadditive which control the cell morphology, reduces static and provideslubrication during the foaming process.

It is a further object of the present invention to lower the cost of apolymeric foam product in a simple and economical manner, such as byusing nano-graphite as a low cost, functional colorant.

Additionally, the present invention provides a process for making aclosed-cell, alkenyl aromatic polymer foam product in whichnano-particle nucleation agents are utilized to control the cellmorphology. The exemplary process includes: 1) heating an alkenylaromatic polymer to the temperature above the glass transitiontemperature of the polymer (for amorphous polymer), or melt point of thepolymer (for crystal polymer) to form a polymer melt; 2) incorporatingan appropriate amount of selected nano-particles (e.g. nano-graphite)into the polymer melt to alter the polymer property and processbehavior, such as rheology, melt strength; 3) incorporating blowingagents into the polymer melt at elevated pressure; 4) incorporatingother additives, such as flame retardants into the polymer melt; and 5)extruding and forming a foam product, typically a rigid insulationboard, under an atmospheric or sub-atmospheric pressure (partial vacuum)to produce a desired cell morphology, characterized by parameters suchas cell size range and distribution, cell orientation and cell wallthickness.

One exemplary embodiment of the present invention provides a process formaking a rigid polymer foam having a mean cell size ranging from severaltens of microns to several hundred microns, preferably around 60microns, by using surface modified hydrophobic nano-particles (e.g.nano-graphite). Conventional foams, in comparison, tend to have a mediancell size of more than 150 microns produced by using conventionalinorganic nucleating agents such as hydrophilic talc. The rigid foamsprepared according to this exemplary embodiment of the inventionexhibited no detectable corrugation and an improvement in compressivestrength of around 30%.

A further exemplary embodiment of the present invention provides aprocess for forming an improved foam structure using a carbon dioxideblowing agent in combination with a nano-scale nucleating agent, such asnano-MMT, to produce a rigid foam having a reduced median cell size andthinner cell walls both to improve mechanical strength and decreasethermal conductivity (thereby increasing the insulation value) of theresulting foam.

The foregoing and other objects, features, and advantages of theinvention will appear more fully hereinafter from a consideration of thedetailed description that follows. It is to be expressly understood,however, that the drawings are for illustrative purposes and are not tobe construed as defining the limits of the invention.

BRIEF DESCRIPTION OF THE DRAWINGS

The advantages of this invention will be apparent upon consideration ofthe following detailed disclosure of the invention, especially whentaken in conjunction with the accompanying drawings wherein:

FIG. 1 is a graphical illustration depicting the density and compressivemodulus of polystyrene foam and polystyrene foams containingnano-graphite;

FIG. 2 is a graphical illustration comparing the rheology of purepolystyrene foam and polystyrene foam containing nano-graphite;

FIG. 3 is a scanning electronic microscope (SEM) image of the foam cellsof the present invention;

FIG. 4 is a scanning electronic microscope (SEM) image of the foam cellwalls and struts;

FIG. 5 is a graphical illustration comparing a polystyrene foam board tothe nano-graphite/polystyrene board of the present invention when bothboards are exposed to UV radiation;

FIG. 6 is a scanning electron microscope (SEM) image of the cell wallstructure of a typical extruded polystyrene (XPS) foam;

FIG. 7 is an SEM image of the cell strut structure of a typical extrudedpolystyrene (XPS) foam;

FIG. 8 is an SEM image of an XPS foam with average cell size of about 81microns produced with about 0.5% of a nano-clay nucleating agent;

FIG. 9 is an optical microscope image of the cell size, cell sizedistribution, and cell orientation (x/z) of an XPS foam with 2%nano-calcium carbonate;

FIG. 10 is an optical microscope image of the cell size, cell sizedistribution, and cell orientation (x/z) of an XPS foam with 3.3% of anano-expanded graphite nucleating agent; and

FIG. 11 is an SEM cell morphology image of an XPS foam sample preparedusing 5% nano-MMT as a nucleating agent and 6% CO₂ as a blowing agent.

DETAILED DESCRIPTION AND PREFERRED EMBODIMENTS OF THE INVENTION

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which the invention belongs. Although any methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of the present invention, the preferred methodsand materials are described herein. All references cited herein,including published or corresponding U.S. or foreign patentapplications, issued U.S. or foreign patents, or any other references,are each incorporated by reference in their entireties, including alldata, tables, figures, and text presented in the cited references. Inthe drawings, the thickness of the lines, layers, and regions may beexaggerated for clarity.

The above objects have been achieved through the development of polymerfoam products which contains nano-graphite to control cell morphologyand act as a gas diffusion barrier. The foam products exhibit improvedthermal insulation (R-values), the nano-graphite acting as an infraredattenuating agent and a cell nucleating agent. The nano-graphite in thefoam also serves as an internal lubricant during processing of the foamand permits the release of surface static during processing of the foam.Foams containing nano-graphite, of the present invention, also haveincreased dimensional stability.

The present invention particularly relates to the production of a rigid,closed cell, polymer foam board prepared by extruding process withnano-graphite, at least one blowing agent and, optionally, otheradditives.

The rigid foamed plastic materials may be made of any such materialssuitable to make polymer foams, which include polystyrenes, polyolefins,polyvinylchloride, polycarbonates, polyetherimides, polyamides,polyesters, polyvinylidene chloride, polymethylmethacrylate,polyurethanes, polyurea, phenol-formaldehyde, polyisocyanurates,phenolics, copolymers and terpolymers of the foregoing, including forexample, styrene-acrylonitrile (SAN) and acrylonitrile-butadiene-styrene(ABS), thermoplastic polymer blends, rubber modified polymers, and thelike. Suitable polyolefins include polyethylene and polypropylene, andethylene copolymers.

A preferred thermoplastic polymer comprises an alkenyl aromatic polymermaterial. Suitable alkenyl aromatic polymer materials include alkenylaromatic homopolymers and copolymers of alkenyl aromatic compounds andcopolymerizable ethylenically unsaturated comonomers. The alkenylaromatic polymer material may further include minor proportions ofnon-alkenyl aromatic polymers. The alkenyl aromatic polymer material maybe comprised solely of one or more alkenyl aromatic homopolymers, one ormore alkenyl aromatic copolymers, a blend of one or more of each ofalkenyl aromatic homopolymers and copolymers, or blends of any of theforegoing with a non-alkenyl aromatic polymer. Suitable polymersgenerally have weight-average molecular weights from about 30,000 toabout 500,000.

Suitable alkenyl aromatic polymers include those derived from alkenylaromatic compounds such as styrene, alpha-methylstyrene, ethylstyrene,vinyl benzene, vinyl toluene, chlorostyrene, and bromostyrene. Minoramounts of monoethylenically unsaturated compounds such as C₂₋₆ alkylacids and esters, ionomeric derivatives, and C₄₋₆ dienes may becopolymerized with alkenyl aromatic compounds. Examples ofcopolymerizable compounds include acrylic acid, methacrylic acid,ethacrylic acid, maleic acid, itaconic acid, acrylonitrile, maleicanhydride, methyl acrylate, ethyl acrylate, isobutyl acrylate, n-butylacrylate, methyl methacrylate, vinyl acetate and butadiene. In one ormore exemplary embodiments, the alkenyl aromatic polymer issubstantially polystyrene (i.e., at least 80%, even 95% polystyrene),and may be composed completely of polystyrene.

The nano-graphite used in this invention has at least one dimension,most likely the thickness of the particle, less than about 100nanometers, which may be measured by X-ray diffraction. Other dimensionsof particles may be less than about 100 microns, less than about 50microns, or less than about 20 microns. The foam may comprise nanosheetsof exfoliated graphite dispersed in the polymeric matrix. Exfoliatedgraphite is graphite that has been intercalated, preferably by anoxidation process, where the atoms or molecules have been inserted intothe inter-planar spacing between the layered planes of carbons, andexpanded. The intercalated graphite is expanded or exfoliated preferablyby brief exposure to high heat to expand the thickness of the graphite.The expanded or exfoliated graphite is then mixed with monomers andpolymerized in situ to form a polymer with a network of nanosheets ofthe exfoliated graphite dispersed therein.

The exfoliated graphite advantageously retains its nanostructure duringthe polymerization process. The expanded or exfoliated graphite iscompressed together into flexible thin sheets. The nano-graphite in thefoam comprises a plurality of nanosheets typically in layers, where eachlayer may comprise few or even a single carbon layer. The nanosheetshave a thickness of between about 10 to several hundred nanometers, withmajority in the range from about 10 to about 100 nanometers. Detailedexplanation of graphite exfoliation may be found in GraphiteIntercalation Compounds I: Structure and Dynamics, H. Zabel; S. A. Solin(1990) and Carbon and Graphite Handbook, C. L. Mantell (1968), which areherein incorporated by reference.

Nano-graphite is added in an amount from preferably greater than 0% toabout 10% by weight, e.g. from about 0.01% to about 10% by weight orabout 0.05% to about 5% by weight, with exemplary preferred ranges fromabout 0.5% to about 5% by weight or from about 0.5% to about 3% byweight or from about 0.05% to about 2.5% by weight.

Blowing agents and other optional additive agents are described below inconnection with the process and/or in examples. Further properties ofthe foam products are also described below.

In another aspect, the present invention relates to a process forpreparing a foam product involving the steps of forming a foamablemixture of (1) polymers having weight-average molecular weights fromabout 30,000 to about 500,000, (2) nano-graphite, as previouslydescribed, (3) at least one blowing agent, and, optionally, (4) otherprocess additives, such as a nucleation agent, flame retardantchemicals, foaming the mixture in a region of atmosphere or reducedpressure to form the foam product. In one embodiment, the polymer ispolystyrene having weight-average molecular weight of about 250,000.

Standard extrusion processes and methods which may be used in theprocess of manufacturing the invention are described in commonly ownedU.S. Pat. No. 5,753,161, which is herein incorporated by reference inits entirety. Detailed descriptions of foaming methods, includingexpansion and extrusion can be found in Plastics Processing DataHandbook (2nd Edition), Rosato, Dominick© 1997 Springer-Verlag which isherein incorporated by reference.

In the extrusion process, an extruded polystyrene polymer, nano-graphitefoam is prepared by twin-screw extruders (low shear) with flat die andplate shaper. Alternatively, a single screw tandem extruder (high shear)with radial die and slinky shaper can be used. Nano-graphite is thenadded into the extruder in an amount from preferably greater than 0% toabout 10% by weight, e.g. from about 0.01% to about 10% by weight orabout 0.05% to about 5% by weight or more preferably from about 0.5% toabout 5% or from about 0.5% to about 3% or from about 0.05% to about2.5% by weight, based on the weight of the polymer along with thepolymer(s) (e.g., polystyrene), a blowing agent, and optionally, otheradditives such as those described below. In exemplary embodiments, anextruded polystyrene polymer foam is prepared by twin-screw extruders(low shear) with flat die and plate shaper. The nano-graphite compoundmay be added into the extruder via multi-feeders, along withpolystyrene, a blowing agent, and/or other additives.

The plasticized resin mixture containing nano-graphite, polymer, andother optional additives is heated to the melt mixing temperature andthoroughly mixed. The melt mixing temperature must be sufficient toplasticize or melt the polymer. Therefore, the melt mixing temperatureis at or above the glass transition temperature or melting point of thepolymer. Generally, the melt mix temperature is from about 200 to about250° C., most preferably about 220 to about 240° C. depending on theamount of nano-graphite.

Next, a blowing agent (described further below) is incorporated to forma foamable gel. The foamable gel is then cooled to a die melttemperature. The die melt temperature is typically cooler than the meltmix temperature, and in exemplary embodiments, is from about 100° C. toabout 130° C., and preferably about 120° C. The die pressure should besufficient to prevent prefoaming of the foamable gel, which contains theblowing agent. Prefoaming involves the undesirable premature foaming ofthe foamable gel before extrusion into a region of reduced pressure.Accordingly, the die pressure varies depending upon the identity andamount of blowing agent in the foamable gel. In exemplary embodiments,the pressure is from about 50 to about 80 bars, most preferably about 60bars. The expansion ratio, foam thickness per die gap, is in the rangeof about 20 to about 70, typically about 60. FIG. 2 illustrates acomparison of viscosity (eta* in Pa-sec) between grade 1600 polystyrenefrom NOVA Chemical, PA and the same polystyrene with 1 wt % ofnano-graphite additive at regular die shear rate range (around 100rad/sec frequency). In the regular die temperature operation range, from115 to 125° C., the viscosity of the polystyrene with nano-graphite ishigher, but is manageable within the operation temperature window.

Any suitable blowing agent and combinations of blowing agents may beused in the practice on this invention. Blowing agents useful in thepractice of this invention may be selected from: 1) organic blowingagents, such as aliphatic hydrocarbons having 1-9 carbon atoms(including, for example, methane, ethane, propane, n-butane, isobutane,isopentane, n-pentane, isopentane, neopentane and cyclopentane) andfully or partially halogenated aliphatic hydrocarbons having 1-4 carbonatoms (see below) and aliphatic alcohols, ketones, esters and ethershaving 1-3 carbon atoms (e.g. methanol, ethanol, n-propanol, andisopropanol; and acetone, methylformate, and dimethylether); 2)inorganic blowing agents, such as carbon dioxide, nitrogen, water, air,argon, nitrogen, and helium; and 3) chemical blowing agents, such asazodicarbonamide, azodiisobutyro-nitrile, benzenesulfonhydrazide,4,4-oxybenzene sulfonyl-semicarbazide, p-toluenesulfonyl, p-toluenesulfonyl semi-carbazide, barium azodicarboxylate, andN,N′-dimethyl-N,N′-dinitrosoterephthalamide and trihydrazino triazine.

Exemplary halogenated aliphatic hydrocarbon blowing agents includefluorocarbons, chlorocarbons and chlorofluorocarbons. Examples ofpartially or fully halogenated fluorocarbons include methyl fluoride,difluoromethane (HFC-32), perfluoromethane, ethyl fluoride (HFC-161),1,2-difluoroethane (HFC-142), 1,1-difluoroethane (HFC-152a),1,1,1-trifluoroethane (HFC-143a), 1,1,1,2-tetrafluoro-ethane (HFC-134a),1,1,2,2-tetrafluoroethane (HFC-134), pentafluoroethane (HFC-125),perfluoroethane, 2,2-difluoropropane (HFC-272fb), 1,1,1-trifluoropropane(HFC-263fb), 1,1,1,3,3-pentafluoropropane (HFC 245fa),1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea), perfluoropropane,1,1,1,3,3-pentafluorobutane (HFC-365mfc), perfluorobutane, andperfluorocyclobutane. Examples of partially halogenated chlorocarbonsand mixed, chlorofluorocarbons for use in this invention include methylchloride, methylene chloride, chlorodifluoromethane (HCFC-22), ethylchloride, 1,1,1-trichloroethane, 1,1,1-trifluoroethane,1,1-dichloro-1-fluoroethane (HCFC-141b), 1-chloro-1,1-difluoroethane(HCFC-142b), 1,1-dichloro-2,2,2-trifluoroethane (HCFC-123) and1-chloro-1,2,2,2-tetrafluoroethane (HCFC-124), pentafluoroethane,dichloropropane, and the like. Examples of fully halogenatedchlorofluorocarbons include trichloromonofluoromethane (CFC-11),dichlorodifluoromethane (CFC-12), trichlorotrifluoroethane (CFC-113),dichlorotetrafluoroethane (CFC-114), chloroheptafluoropropane, anddichlorohexafluoropropane.

Particularly useful blowing agents include 1-chloro-1,1-difluoroethane(HCFC-142b), 1,1,1,2-tetrafluoro-ethane (HFC-134a), carbon dioxide, and1,1-difluoroethane (HFC-152a); and blends of these: e.g. HCFC-142b withcarbon dioxide, HFC-134a with carbon dioxide, carbon dioxide withethanol, carbon dioxide with water, and HFC-134a with HFC-152a. About50% of the HFC-134a blowing agent and about 50% of the HFC-152a blowingagent may be present in the composition. Both components are based onthe weight of the polymer. However, for low density, thick products, theamount of HFC-152a may be increased up to about 60% or more based on theweight of the polymer.

In the present invention, it is preferable to use about 6 to about 14%,preferably about 11%, by weight based on the weight of the polymer ofthe blowing agent (e.g. cyclopentane). If used, it is also preferred toadd about 0 to about 4% ethanol and/or about 3 to about 6%, preferablyabout 3.5% carbon dioxide. All percentages are based on the weight ofthe polymer.

Optional additives may be incorporated in the extruded foam product andmay include, but are not limited to, additional infrared attenuatingagents, cell size enlarging agents, plasticizers, flame retardantchemicals, pigments, elastomers, extrusion aids, antioxidants, fillers,antistatic agents, UV absorbers, citric acids, nucleating agents,surfactants, processing aids, and mold release aids. These optionaladditives may be included in any amount to obtain desiredcharacteristics of the foamable gel or resultant extruded foam productsand/or to improve the processing of the foam or modify one or moreproperties of the resulting foam. Preferably, optional additives areadded to the resin mixture but may be added in alternative ways to theextruded foam manufacture process.

Although the polymer foams manufactured according to the presentinvention may have structures exhibiting both closed cells and opencells, preferred foam compositions will have at least 90 percent closedcells as measured according to ASTM D2856-A. Exemplary embodiments ofpolymer foam products manufactured according to the present inventioncan exhibit densities of from about 10 to about 500 kg/m³, but will morepreferably have densities of from about 20 to about 60 kg/m³ whenmeasured according to ASTM D-1622. For a preferred rigid, foaminsulation board as described herein, the density is generally about20-80 kg/m³ (about 1.2-5 pcf), typically about 22-48 kg/m³ (about 1.4 toabout 3 pcf); and is about ⅛ to about 12 inches thick, typically about 1to about 4 inches thick. The resulting board exhibits an R-value (perinch) of from about 3 to about 8.

As mentioned above, the nano-graphite in the foam controls cellmorphology. The nano-scale graphite acts as a nucleating agent in thefoaming process. The cell morphology includes parameters such as cellmean size, cell anisotropic ratio or cell orientation, cell density,cell size distribution, cell wall thickness, cell strut effectivediameter, open/closed cell ratio, cell shape, such as pentagonaldodecahedral, rhombic dodecahedron, tetra dodecahedral (with curvedsurface), and other models of cells such as bi-cell and cell-in-cellmodels. Within these cell morphology parameters, cell mean size, cellwall thickness, cell strut effective diameter, and cell orientation arekey parameters for determining the foam physical properties of closedcell foams.

The invention uses nano-particles such as nano-graphite and theabove-described extrusion process to control the cell size, cell wallthickness, strut effective diameter, and cell orientation of the foamproducts within a relatively broad range. As discussed above, theparticle size of the present nano-particle cell size controlling agent(e.g. nano-graphite) is typically no greater than 100 nanometers in atleast one dimension, typically the thickness dimension. Additionally,the nano-particle may be an organic or inorganic material either with orwithout surface modification. Conventional polymer foams tend to exhibita cell mean size in the range between about 120 and 280 microns. Byutilizing the nano-particle technology according to the presentinvention, it is possible to manufacture polymer foam structures havinga cell mean size from several tens of microns to several hundredmicrons.

FIG. 3 is a scanning electron microscope (SEM) image of the foamincluding 1% nano-graphite in polystyrene foam. The average cell size ofthe foam without any other nucleating agent such as talc is around 220microns; orientation in the x/z direction=1.26 (x 0.254, y 0.205, z0.201 mm) FIG. 4 is an SEM image of the cell walls and struts of thefoam product. The polystyrene foam contains 1% nano-graphite. Thethickness of the cell walls is about 0.86 microns, the strut diameter isabout 3.7 microns.

FIG. 5 illustrates the UV protectability of a polystyrene foam boardincluding the nano-graphite of the present invention when the board isexposed to UV radiation. The test method used is a QUV test, followed bycolor measurement. Test methods and material standards for the QUV testinclude ISO 4982-1 Plastics, ASTM G-151, ASTM G-154, ASTM G53, BritishStandard BS 2782, Part 5, Method 540B, and SAE J2020, JIS D0205. Alltest methods and standards cited above are herein incorporated byreference in their entireties. The color measurements are made on theL*a*b scales. The L scale, from 0 to 100, represents a black to whiterelationship. The nano-graphite foam with grey color was almost nochange from an extended UV exposure for more than 100 days. The a and bscale, from 1 to −1, represent the different color changes: from red togreen, and from yellow to blue. Slight changing of color has beenobserved after more than 90 days UV exposure for the nano-graphite foamboard.

Having generally described this invention, a further understanding canbe obtained by reference to certain specific examples illustrated belowwhich are provided for purposes of illustration only and are notintended to be all inclusive or limiting unless otherwise specified.

EXAMPLES

A series of exemplary and comparative foam structures were prepared andevaluated to determine cell morphology, i.e., cell size, cell wallthickness (FIG. 6), effective diameter of cell strut (FIG. 7), cellanisotropy ratio, and certain other properties related to the foam cellmorphology. In particular, FIGS. 6 and 7 show the SEM imagines of thecell wall and strut structure of a typical extruded polystyrene (XPS)foam. If a polymer foam is ideally depicted as a close wall ofpentagonal dodecahedral cells in a uniform size, the cell wall thicknessand the strut effective diameter then depend primarily on the density ofthe foam and the cell size.

The physical properties tested included one or more of density,compressive strength, thermal conductivity, aged thermal insulationvalue, thermal dimensional stability. In connection with these examples,cell size was measured according to ASTM D3576; density was measuredaccording to ASTM D1622; thermal conductivity was measured according toASTM C518; compressive strength was measured according to ASTM D1621;and thermal dimensional stability was measured according to ASTM D2126.

The foam structures were made with a twin co-rotated screw extrudercomprising a pair of extruder screw, a heating zone mixer, a blowingagent injector, a cooler, a die and a shaper in accord with theoperational conditions listed below in Table 1. The conditions set forthin Table 1 are applicable to Examples 1-6. Unless otherwise indicated,the polymer utilized in preparing the example foam compositions was anAtoFina granular polystyrene having a weight average molecular weight(M_(w)) of about 250,000, and melt index of about 3.1 μm per 10 minutes.

TABLE 1 LMP Co-rotating Twin Leistritz MIC 27 Screw Extruder with GL/400Co-rotating Static Cooler Twin Screw Extruder Die/Shaper Flat face die/20 × 2 mm Shaper plate Flat Slot Die Forming AtmosphereAtmosphere/Vacuum Atmosphere Throughput - kg/hr. 100-200  6-10 Wt. % ofHCFC-142b 10.5-11.5 Wt. % of HCFC-142b/22 Wt. % of CO₂ Mixing 210-230200-220 Temperature - ° C. Extruder Pressure - 13000-17000 6900-8300 kPa(psi) (1950-2400) (1000-1200) Die Melt 117-123 130-160 Temperature - °C. Die Pressure - 5400-6600 5500-8000 kPa (psi) (790-950)  (800-1150)Line Speed - m/hr 108-168 90-80 (ft/min) (5.9-9.2)  (5-10) Die Gap - mm0.6-0.8 2 Vacuum - kPa  0-3.4 Atmosphere (inch Hg) (0 to 16)

Example 1

Polystyrene foams were prepared both with (7347) and without (7346) a2.5% nano-particle loading using an LMP extruder. The nano-particle usedto prepare this Example was an organoclay, specifically grade Nano-MMT20A from Southern Clay Products Inc., that was melt compounded with apolystyrene polymer, specifically grade CX5197 from AtoFina, to form amelt polymer. The nano-particles exhibited an intercalated nano-MMTlayer structure when examined using X-ray diffraction. The comparisonsample did not include any nano-particles, but incorporated 0.8% talcloading as the nucleating agent. The comparison sample exhibited anaverage cell size of around 186 microns while the exemplary exampleutilizing the nano-particle foam exhibited a significantly reducedaverage cell size of around 60 microns. The exemplary example alsoexhibited a cell wall thickness of around 0.5 micron, and a struteffective diameter of around 5 microns. As reflected below in Table 2,the exemplary foam composition did not exhibit corrugation, wasprocessed without undue process difficulty and provided improvements incompressive strength of around 30%.

TABLE 2 Nano- Average Cell Particle Cell Anisotropic Density StrengthThickness Sample Wt. % micron Ratio* kg/m³ kPa mm 7346 0 186 0.949 29.28286 37 7347 2.5 62 0.968 32 372 26 *Cell anisotropic ratio: K =z/(x.y.z)^(1/3) where, x, an average cell size in the longitudinal(extruding) direction, y, cell size in the transverse direction, and z,cell size in the board thickness direction

Example 2

Sample foams (7349) were produced according to the process outlined inExample 1, but using 0.5% of an intercalated nano-MMT in a polystyrenecomposition to produce an exemplary foam having a density of about 26.5kg/m³, a thickness of about 38 mm and a width of about 600 mm. Thereduction in the amount of nano-MMT incorporated into the compositionresulted in a slightly increased cell size, about 83 microns (FIG. 8),compared with Example 1, while maintaining improved strength, 329 kPa,over the comparative foam compositions.

Example 3

Foams (7790) were prepared using a nano-particle loading of 2%nano-calcium carbonate from Ampacet, along with 1% talc as an additionalnucleating agent and 1% of stabilized hexabromocyclododecone as fireretardant agent in a LMP extruder. The nano-calcium carbonate particleswere typically elongated, having average dimensions of 80 nm×2 μm, andwere provided in a 50% master batch composition in combination with anolefinic copolymer carrier resin. The rest of formulation waspolystyrene: 80% Nova 1220 (Melt Index=1.45) and 16% Nova 3900 (MeltIndex=34.5). The exemplary foam produced was 28 mm thick, 400 mm wideand had an average cell size of 230 microns with a cell orientation—theratio of the cell dimension in the extrusion direction to the celldimension in the thickness direction (x/z)—as high as 1.54 (see FIG. 9).

Example 4

Foams (7789) were produced as in Example 3, but used 3.3% intercalatedexpanded nano-graphite from Superior Graphite Company as thenano-particles. The expanded nano-graphite included nano-sheets ofgraphite having thicknesses ranging from about 10 to about 100 nm andwidths of around 3 p.m. The exemplary foam exhibited substantially thesame thickness, width, and density (49 kg/m³) as Example 3, but had asmaller average cell size of 166 microns and cell orientation value of1.21 (see FIG. 10). The thermal conductivity of this foam is as low as0.14 K·m²/W for samples after being aged for 20 days.

Example 5

Foams (7289, 7291) were prepared using a Leistritz extruder to producesamples having a thickness of around 10 mm, a width of around 50 mm, anda density of around 46 kg/m³. Both samples with 0.5% of talc asnucleating agent, and 10% of HCFCl42b/22 as blowing agent. Somecharacters of cell morphology are summarized as Table 3.

TABLE 3 Strut Nano- Average Cell Cell Wall Effective Particle* CellOrientation Cell Size Thickness Diameter Sample Wt. % micron x/z x y zmicron micron 7289 0 341 0.99 355 359 339 1.8 4.2 7291 5 174 0.95 165183 173 0.8 5.1

Example 6

Foams (7293, 7294) were prepared as in Example 5, but using 6 wt % ofcarbon dioxide as the blowing agent and 0.2 wt % of talc as aconventional nucleating agent. Some characteristics of the resultingcell morphologies (FIG. 11) are summarized below in Table 4.

TABLE 4 Strut Nano- Average Cell Cell Wall Effective Particle* CellOrientation Cell Size Thickness Diameter Sample Wt. % micron x/z x y zmicron micron 7293 0 380 0.92 355 396 388 1.4 3 7294 5 146 0.76 146 121158 0.3 5.4

Example 7

In the following samples and control samples, rigid polystyrene foamboards are prepared by a twin screw LMP extruder with flat die andshaper plate; and a two single screw tandem extruder with radial die andslinky shaper. A vacuum may also be applied in both of the abovedescribed pilot and manufacturing lines.

Table 5 shows the process conditions for samples in a twin screwextruder for making foam boards having a width of 16 inches and athickness of one inch.

TABLE 5 Samples on Table 8 Wt. % of nano-graphite 1 to 5 Wt. % of talc0.5-1.5 Wt. % of nano-carbon black 0 to 6 Wt. % of mica 0 to 4 Wt. % ofHCFC-142b  11 Wt. % of CO₂  0 Extruder Pressure, Kpa (psi) 13000-17000(1950-2400) Die Melt Temperature, (° C.) 117-123 Die Pressure, Kpa (psi)5400-6600 (790-950) Line Speed, m/hr (ft/min) 110-170  (6-9.5)Throughput, kg/hr 100 Die Gap, mm 0.6-0.8 Vacuum KPa (inch Hg)  0-3.4 (0 to 16)

The thickness of nano-graphite used was confirmed by X-ray diffractionto be 29.7 nm, and 51 nm after compounding with about 60 wt % ofpolystyrene. Carbon black was not part of mix with nano-graphite due toits poor process ability and high smoke density during fire test.

The results of above examples are shown in Table 6. All R-values andcompressive strength are tested after the samples aged for 180 days

TABLE 6 Aged R-value Density Compressive Nano- K · m2/K Kg/m3 Strengthgraphite Run # (F · ft2 · hr/Btu) (pcf) psi Wt % Control 0.029 27.68 NA0 sample (5.05) (1.73) 696-2 0.025 28.64 21.55 1 X8234 (5.82) (1.79)696-4 0.024 30.72 22.67 3 X8235 (6.03) (1.92) 692-2 0.025 27.84 25.69 1X8207 (5.77) (1.74) 692-3 0.024 28.8 27.27 2 X8208 (5.94) (1.80) 692-40.024 28.96 26.87 3 X8209 (6.00) (1.81)

As shown from above samples, the addition of nano-graphite in foamingprocessing, preferably about 1% to about 3% by weight of the polymer hasprofound effect on the thermal resistance property. The range of theR-value was determined to be between about 5.7 and about 6.0 per inch.

Example 8

Table 7 compares the operating conditions between batch foaming andtraditional low-density foam extrusion.

TABLE 7 Comparison of Operating Conditions between Batch and ExtrusionFoaming Operating conditions Extrusion Batch Foaming Temperature (° C.)100~140  120 Pressure (psi) 1000~2000 2000 dP/dt (Pa/sec) 10⁶   10⁶

Prior to batch foaming, the polymerized nano-graphite/polystyrenecompound is heated and compressed into a solid shape. The solid sheet iscut into small pieces according to the size of pressure vessel, such as77×32×1 mm. The solid sheet specimen is then placed in a mold and foamedin a high-pressure vessel at about 80 to about 160° C., typically about120° C. and about 500 to about 4000 psi, typically about 2000 psi. Thesolid sheet remains in the pressurized vessel for about 8 to about 50hours, typically about 12 hours, after which the pressure in the vesselwas released quickly (about 12 seconds) for foaming.

The nano-graphite/polystyrene foam of the batch foaming samples wereevaluated to determine the amount infrared radiation transmitted throughthe foam. As infrared light is the major form of thermal radiation.

A piece of batch-foamed sample containing polystyrene and 3% graphite,and two other comparison samples containing polystyrene or polystyreneand 5% nano-clay were selected. On one side of the foam sample a lightsource of infrared laser was placed. On the other side of the sample,either a detector was placed to record the transmission light intensityor a temperature camera was placed to monitor the surface temperaturechange. The results are summarized in Table 8.

TABLE 8 Infrared Light Transmission Through foam samples of polystyrene(PS), polystyrene and 5% nano-clay (PS/5% clay), and polystyrene and 3%nano-graphite (PS/3% graphite) IR Transmission Emissive ReceivedIntensity (watts) Intensity Intensity % Trans PS (control sample) 0.50.05 10%  PS/5% MHABS* 0.5 0.02 4% PS/3% milled graphite worms 0.5 0.012% *in-situ polymerized compound with 5% of reactive cationicsurfactant, 2-methacryloyloxyethylhexadecyldimethyl ammonium bromide(MHAB) treated Na+ montmorillonite with 95% styrene monomer

As shown in Table 8, 10% of the light transmits through the pure PS foamsample, while only 4% through the PS/5% clay foam sample and only 2%through the PS/3% graphite sample. Both clay and graphite have theattenuation effect on the infrared light, however, as shown in the abovetable, PS/3% graphite has considerably better transmission attenuation.

The temperature of the PS/graphite sample, on the side of the sampleopposite to the light source, was slightly elevated, having an increaseof about 2-3° F. after 60 seconds of exposure (Table 9). There was noobvious change in surface temperature for foam samples of pure PS(control sample) and PS with MHABS nano-clay. As such, PS/graphite foamattenuates thermal radiation and enhances the heat solid conduction.Further, by improved graphite dispersion and concentration, these trendsare expected to be more significant.

TABLE 9 Temperature change for foam samples of PS, PS/5% clay, and PS/3%graphite on the surface opposite to the light source IR CameraTemperature at Interval Time in Seconds 0 10 20 30 40 50 60 PS (controlsample) 78.4° F. 78.4° F. 78.7° F. 78.8° F. 78.4° F. 78.5° F. 78.5° F.PS/5% MHABS 79.2° F. 79.2° F. 79.5° F. 79.6° F. 79.4° F. 79.5° F. 79.6°F. PS/3% milled graphite worms 80.6° F. 81.2° F. 81.7° F.   82° F. 82.6°F. 82.8° F.   83° F.

The invention of this application has been described above bothgenerically and with regard to specific embodiments. Therefore, it is tobe understood that a wide variety of alternatives known to those ofskill in the art can be selected within the generic disclosure.

1. A polymeric foam material comprising: foam structures formed from apolymer, at least one blowing agent, and nano-graphite particles havinga size, in at least one dimension, of less than about 100 nanometers;wherein said foam structures comprise cell walls and struts that definecells having morphological parameters.
 2. The polymeric foam material ofclaim 1, wherein the nano-graphite is present in an amount from about0.01% to about 10% by weight based on the polymer.
 3. The polymeric foammaterial of claim 2, wherein the nano-graphite is present in an amountfrom about 0.05% to about 5% by weight based on the polymer.
 4. Thepolymeric foam material of claim 1, wherein said nano-graphite isselected from the group consisting of nanosheets of graphite,intercalated nano-graphite, exfoliated nano-graphite and expandednano-graphite.
 5. The polymeric foam material of claim 1, wherein saidnano-graphite is an intercalated nano-graphite.
 6. The polymeric foammaterial of claim 1, wherein said nano-graphite is an exfoliatednano-graphite.
 7. The polymeric foam material of claim 1, wherein saidnano-graphite is an expanded nano-graphite.
 8. The polymeric foammaterial of claim 1, wherein said nano-graphite comprises nanosheets. 9.The polymeric foam material of claim 8, wherein said nanosheets have athickness between about 10 to about 100 nanometers.
 10. The polymericfoam material of claim 1, wherein said cells have a mean cell size offrom several tens of microns to several hundred microns.
 11. Thepolymeric foam material of claim 8, wherein at least about 90% of saidcells are closed cells.
 12. The polymeric foam material of claim 1,wherein the nano-graphite is present in an amount greater than 0% toabout 10% by weight based on the polymer.
 13. The polymeric foammaterial of claim 4, wherein the nano-graphite is present in an amountfrom about 0.5% to about 3.0% by weight based on the polymer.
 14. Thepolymeric foam material of claim 1, wherein said polymer is selectedfrom the group consisting of: alkenyl aromatic homopolymers, alkenylaromatic homopolymers and copolymers, or blends of any of the foregoingwith a non-alkenyl aromatic polymer.
 15. The polymeric foam material ofclaim 14, wherein said polymer includes an alkenyl aromatic polymerderived from monomers selected from the group consisting of: styrene,alpha-methylstyrene, chlorostyrene, bromostyrene, ethylstyrene, vinylbenzene, and vinyl toluene.
 16. The polymeric foam material of claim 15,wherein said polymer is at least 80% polystyrene.
 17. The polymeric foammaterial of claim 2, wherein said polymer is selected from polystyrenes,polyolefins, polyvinylchloride, polycarbonates, polyetherimides,polyamides, polyesters, polyvinylidene chloride, polymethylmethacrylate,polyurethanes, polyurea, phenol-formaldehyde, polyisocyanurates,phenolics, copolymers and terpolymers of the foregoing, thermoplasticpolymer blends rubber modified polymers and combinations thereof. 18.The polymeric foam material of claim 1, wherein at least one blowingagent is selected from the group consisting of organic, inorganic andchemical blowing agents.
 19. The polymeric foam material of claim 18,wherein at least one blowing agent is selected from the group consistingof: aliphatic hydrocarbons having 1-9 carbon atoms and fully orpartially halogenated aliphatic hydrocarbons having 1-4 carbon atoms.20. The polymeric foam material of claim 18, wherein said blowing agentis selected from the group consisting of: 1-chloro-1,1-difluoroethane(HCFC-142b), HCFC-134a, carbon dioxide, blends of HCFC-142b with carbondioxide, HCFC-134a with carbon dioxide, carbon dioxide with ethanol, orcarbon dioxide with water.
 21. The polymeric foam material of claim 18,wherein at least one blowing agent is selected from the group consistingof methane, ethane, propane, n-butane, isobutane, isopentane, n-pentane,isopentane, neopentane, cyclopentane, methanol, ethanol, n-propanol, andisopropanol.
 22. The polymeric foam material of claim 18, wherein atleast one blowing agent is selected from the group consisting of:difluoromethane (HFC-32), ethyl fluoride (HFC-161), 1,2-difluoroethane(HFC-142), 1,1-difluoroethane (HFC-152a), 1,1,1-trifluoroethane(HFC-143a), 1,1,1,2-tetrafluoro-ethane (HFC-134a),1,1,2,2-tetrafluoroethane (HFC-134), pentafluoroethane (HFC-125),2,2-difluoropropane (HFC-272fb), 1,1,1-trifluoropropane (HFC-263fb),1,1,1,3,3-pentafluoropropane (HFC 245fa),1,1,1,2,3,3,3-heptafluoropropane (HFC-227ea),1,1,1,3,3-pentafluorobutane (HFC-365mfc), chlorodifluoromethane(HCFC-22), 1,1-dichloro-1-fluoroethane (HCFC-141b),1-chloro-1,1-difluoroethane (HCFC-142b),1,1-dichloro-2,2,2-trifluoroethane (HCFC-123) and1-chloro-1,2,2,2-tetrafluoroethane (HCFC-124),trichloromonofluoromethane (CFC-11), dichlorodifluoromethane (CFC-12),trichlorotrifluoroethane (CFC-113), dichlorotetrafluoroethane (CFC-114),and mixtures thereof.
 23. The polymeric foam material of claim 2,wherein at least one blowing agent is selected from1,1,1,2-tetrafluoroethane (HFC-134a), 1,1-difluoroethane (HFC-152a),1,2-difluoroethane (HFC-142) and mixtures thereof.
 24. The polymericfoam material of claim 1, wherein said foam material has a density offrom about 10 to about 500 kg/m³.
 25. The polymeric foam material ofclaim 24, wherein said foam material has a density of from about 20 toabout 60 kg/m³.
 26. The polymeric foam material of claim 1, furthercomprising an additive selected from the group consisting of: flameretardants, mold release aids, pigments and fillers.
 27. The polymericfoam material of claim 1, wherein said foam material is a rigid, closedcell board.
 28. The polymeric foam material of claim 27, wherein saidrigid, closed cell board is formed by extrusion.
 29. The polymeric foammaterial of claim 27, wherein said rigid, closed cell board is aninsulating foam board having a thickness from about ⅛ inch to about 12inches.
 30. The polymeric foam material of claim 27, wherein said rigid,closed cell board is an insulating foam board having an R-value per inchof about 3 to about
 8. 31. A rigid foam insulation board comprising thepolymeric material of claim 2, wherein the polymeric material isextruded into a rigid board.
 32. A rigid foam insulation boardcomprising the polymeric material of claim 15, wherein the polymericmaterial is extruded into a rigid board.
 33. A rigid foam insulationboard comprising the polymeric material of claim 19, wherein thepolymeric material is extruded into a rigid board.
 34. A rigid foaminsulation board comprising the polymeric material of claim 24, whereinthe polymeric material is extruded into a rigid board.
 35. A rigid foaminsulation product comprising: a polymeric material formed from apolymer, at least one blowing agent, and nano-graphite particlesselected from the group consisting of nanosheets of graphite,intercalated nano-graphite, exfoliated nano-graphite and expandednano-graphite, and having a size, in at least one dimension, of lessthan about 100 nanometers; wherein said polymeric material comprisescell walls and struts that define cells having morphological parameters;and wherein the polymeric material is extruded into a rigid product. 36.The rigid foam insulation product of claim 35, wherein saidnano-graphite is present in said board in an amount from about 0.01% toabout 10% by weight based on said polymer.
 37. The rigid foam insulationproduct of claim 36, wherein said nano-graphite is present in said boardin an amount from about 0.05% to about 5% by weight based on saidpolymer.
 38. A rigid foam insulation product of claim 35 wherein saidpolymeric material polymer includes an alkenyl aromatic polymer derivedfrom monomers selected from the group consisting of: styrene,alpha-methylstyrene, chlorostyrene, bromostyrene, ethylstyrene, vinylbenzene, and vinyl toluene.
 39. A rigid foam insulation product of claim38 wherein said polymeric material polymer is at least 80% polystyrene.40. The rigid foam insulation product of claim 35, wherein at least oneblowing agent is selected from the group consisting of: aliphatichydrocarbons having 1-9 carbon atoms and fully or partially halogenatedaliphatic hydrocarbons having 1-4 carbon atoms.
 41. The rigid foaminsulation product of claim 40, wherein at least one blowing agent isselected from 1,1,1,2-tetrafluoroethane (HFC-134a), 1,1-difluoroethane(HFC-152a), 1,2-difluoroethane (HFC-142) and mixtures thereof.
 42. Therigid foam insulation product of claim 35, wherein said insulationproduct is a board having a thickness from about ⅛ inch to about 12inches.
 43. The rigid foam insulation board of claim 42 wherein theR-value per inch of said board is from about 3 to about
 8. 44. The rigidfoam insulation board of claim 42, further comprising one or moreadditives selected from infrared attenuating agents, plasticizers, flameretardant chemicals, elastomers, extrusion aids, antioxidants, pigments,fillers, antistatic agents and UV absorbers.
 45. The rigid foaminsulation product of claim 35, wherein said nano-graphite comprisesnanosheets of graphite having a thickness between about 10 to about 100nanometers.
 46. The rigid foam insulation product of claim 35, whereinat least about 90% of which cells are closed cells
 47. A method formaking an extruded polymer foam product comprising: mixing a resinmixture including a polymer and nano-graphite; wherein saidnano-graphite has a size, in at least one dimension, that is less thanabout 100 nm; heating said resin mixture to a mixing temperature;incorporating at least one blowing agents into the resin mixture under apressure sufficient to prevent pre-foaming of the gel; cooling the gelto a die temperature; and extruding the gel through a die to a region oflower pressure to form the foam.
 48. The method of claim 47, whereinsaid nano-graphite is present in said resin mixture in an amount greaterthan 0.01% to about 10% by weight based on the polymer.
 49. The methodof claim 48, wherein said nano-graphite is selected from the groupconsisting of nanosheets of graphite, intercalated nano-graphite,exfoliated nano-graphite and expanded nano-graphite.
 50. The method ofclaim 47, wherein said nano-graphite is an intercalated nano-graphite.51. The method of claim 47, wherein said nano-graphite is an exfoliatednano-graphite.
 52. The method of claim 47, wherein said nano-graphite isan expanded nano-graphite.
 53. The method of claim 47, wherein saidnano-graphite comprises nanosheets of graphite having a thickness ofabout 10 to about 100 nanometers.
 54. The method of claim 47, whereinsaid polymeric material polymer includes an alkenyl aromatic polymerderived from monomers selected from the group consisting of: styrene,alpha-methylstyrene, chlorostyrene, bromostyrene, ethylstyrene, vinylbenzene, and vinyl toluene.
 55. The method of claim 54, wherein saidpolymeric material polymer is at least 80% polystyrene.
 56. The methodof claim 47, wherein at least one blowing agent is selected from thegroup consisting of: aliphatic hydrocarbons having 1-9 carbon atoms andfully or partially halogenated aliphatic hydrocarbons having 1-4 carbonatoms.
 57. The method of claim 56, wherein at least one blowing agent isselected from 1,1,1,2-tetrafluoroethane (HFC-134a), 1,1-difluoroethane(HFC-152a), 1,2-difluoroethane (HFC-142) and mixtures thereof.
 58. Themethod of claim 47, wherein at least one blowing agent is selected from1,1,1,2-tetrafluoroethane (HFC-134a), 1,1-difluoroethane (HFC-152a),water, carbon dioxide, ethanol and mixtures thereof.
 59. The method ofclaim 47, wherein said extruded foam product is a board having athickness from about ⅛ inch to about 12 inches.
 60. The method of claim59, wherein the R-value per inch of said extruded foam product is fromabout 3 to about
 8. 61. The method of claim 47, further comprising thestep of mixing one or more additives selected from the group consistingof infrared attenuating agents, plasticizers, flame retardant chemicals,pigments, elastomers, extrusion aids, antioxidants fillers, antistaticagents and UV absorbers into said mixture.
 62. The method of claim 47,wherein the polymer mixing temperature is from about 200° C. to about250° C., and the die temperature is from about 100° C. to about 130° C.63. The method of claim 47, wherein the step of incorporating at leastone blowing agent into the resin mixture under a pressure sufficient toprevent pre-foaming of the gel is done at a pressure from about 50 toabout 80 bars.
 64. The method of claim 47, wherein the foam expansionratio is from about 20 to about
 70. 65. An extruded, polymeric foamproduct manufactured according to the method of claim 47.